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Projets de recherche
ALLEMAGNE
Nordrhein-Westfalen
AACHEN
Shaping human nociceptor excitability via activation of sodium channel Nav1.9. Building a basis for innovative pain therapies
Universitätsklinikum Aachen
Institut für Physiologie
AUTRICHE
STEIERMARK
GRAZ
ENISNIP : European Network on Inherited Sensory Neuropathies and Insensitivity to Pain - AT
CMT Austria
AUTRICHE
WIEN
WIEN
ENISNIP : European Network on Inherited Sensory Neuropathies and Insensitivity to Pain - AT
Medizinische Universität Wien
ESPAGNE
Comunidad Valenciana
VALENCIA
Genotypical and phenotypical characterization in a series of patients with late-onset hereditary neuropathies
Hospital Universitario y Politécnico La Fe
Unidad de Patología Neuromuscular
ESPAGNE
Cataluña
BARCELONA
Advanced genomics and lipidomics for identifying novel causes of inherited movement disorders
Instituto de Química Avanzada de Cataluña
Unidad de Investigación en Moléculas Bioactivas
ESPAGNE
País Vasco
SAN SEBASTIÁN
Advanced genomics and lipidomics for identifying novel causes of inherited movement disorders
Instituto de Investigación Sanitaria Biodonostia
Área de Neurociencias
ESPAGNE
Cataluña
BARCELONA
Igenco: In-Depth genomics and cross-omics analysis for undiagnosed rare diseases on a user-friendly collaborative platform
ISGlobal - Instituto de Salud Global de Barcelona
Programa de investigación en Enfermedades no transmisibles y medio ambiente
ESPAGNE
Madrid
MADRID
RAREGenomics: Network of Genomic, Functional, Clinical and Therapeutic Resources for the Study of Rare Neurological Diseases
Hospital Universitario Fundación Jiménez Díaz
Servicio de Genética Clínica
FRANCE
NOUVELLE AQUITAINE
LIMOGES
Développement d'un traitement à nanoparticules à base de curcumine pour les patients atteints de neuropathies périphériques
Université de Limoges
Équipe Maintenance Myélinique et Neuropathies Périphériques (MMNP)
CANADA
Colombie-Britannique
VICTORIA
Silent Genomes: Reducing health care disparities and improving diagnostic success for children with genetic diseases from Indigenous populations
University of Victoria
Community Genetics Research Program/Island Medical Program
CANADA
Ontario
TORONTO
Beyond the Genome: Transcriptome Based Diagnostics for Rare Diseases and Cancer
Hospital for Sick Children, Research Institute
ESPAGNE
Madrid
MADRID
Identification of new genes causing rare diseases in pediatric patients, searching of genetic pharmacological targets, and drugs discovery, the steps for a personalized medicine
Instituto de Investigación Hospital 12 de Octubre
Grupo de investigación en enfermedades raras, mitocondriales y neuromusculares
ETATS-UNIS
Washington
ADDRESS: NOT PROVIDED - US
A powerful web-based discovery platform for rare disease genetics
Institution: Information not provided - US
FRANCE
ILE-DE-FRANCE
PARIS
La surexpression du gène de la neuroglobine : un outil prometteur pour traiter un large spectre de troubles neurologiques grâce à sa capacité à préserver de manière sûre et durable l'intégrité mitochondriale
Institut National de la Santé et de la Recherche Médicale
ITALIE
LAZIO
ROMA
Diverse rare diseases caused by functional dysregulation of Rho GTPase-related proteins
ISS - Istituto Superiore di Sanità
Centro Nazionale Malattie Rare
Projets de recherche multicentriques
- Azienda Ospedaliera di Padova
- Clinica Pediatrica
- Haukeland University Hospital
ITALIE
VENETO
PADOVA
Brains for brain: research group of the European task force on brain and neurodegenerative lysosomal storage diseases
NORVEGE
Vestlandet
BERGEN